A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592637



Internal ID16380046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177577305..177584329hg38UCSC Ensembl
Innerchr3:177295093..177302117hg19UCSC Ensembl
Innerchr3:178777787..178784811hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg387025
hg197025
hg187025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8752n54
Supporting Variantsnssv981777
Samples
Known GenesLINC00578
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592637
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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